-
1
-
-
33746289399
-
-
note
-
The content of the information discussed herein does not necessarily reflect the position or the policy of the federal government of the United States of America, and no official endorsement should be inferred.
-
-
-
-
2
-
-
0001004984
-
-
a) Y.-C. Yang, J. A. Baker, J. R. Ward, Chem. Rev. 1992, 92, 1729;
-
(1992)
Chem. Rev.
, vol.92
, pp. 1729
-
-
Yang, Y.-C.1
Baker, J.A.2
Ward, J.R.3
-
5
-
-
33746307407
-
-
note
-
-1.
-
-
-
-
7
-
-
0033451222
-
-
N. B. Munro, S. S. Talmage, G. D. Griffin, L. C. Waters, A. P. Watson, J. F. King, V. Hauschild, Environ. Health Perspect. 1999, 107, 933.
-
(1999)
Environ. Health Perspect.
, vol.107
, pp. 933
-
-
Munro, N.B.1
Talmage, S.S.2
Griffin, G.D.3
Waters, L.C.4
Watson, A.P.5
King, J.F.6
Hauschild, V.7
-
8
-
-
0001462624
-
-
Y.-C. Yang, F. J. Berg, L. L. Szafraniec, W. T. Beaudry, C. A. Bunton, A. Kumar, J. Chem. Soc. Perkin Trans. 2 1997, 607.
-
(1997)
J. Chem. Soc. Perkin Trans. 2
, pp. 607
-
-
Yang, Y.-C.1
Berg, F.J.2
Szafraniec, L.L.3
Beaudry, W.T.4
Bunton, C.A.5
Kumar, A.6
-
9
-
-
33746319216
-
-
note
-
- ion reacts with phosphoniothioates to give exclusive P-S cleavage, although these reactions are not catalytic and are carried out under alkaline conditions.
-
-
-
-
10
-
-
0037870451
-
-
a) J. S. Tsang, A. A. Neverov, R. S. Brown, J. Am. Chem. Soc. 2003, 125, 7602;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 7602
-
-
Tsang, J.S.1
Neverov, A.A.2
Brown, R.S.3
-
11
-
-
18444412899
-
-
b) T. Liu, A. A. Neverov, J. S. W. Tsang, R. S. Brown, Org. Biomol. Chem. 2005, 3, 1525;
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 1525
-
-
Liu, T.1
Neverov, A.A.2
Tsang, J.S.W.3
Brown, R.S.4
-
12
-
-
10644240146
-
-
c) J. S. W. Tsang, A. A. Neverov, R. S. Brown, Org. Biomol. Chem. 2004, 2, 3457;
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 3457
-
-
Tsang, J.S.W.1
Neverov, A.A.2
Brown, R.S.3
-
13
-
-
6344237119
-
-
d) W. Desloges, A. A. Neverov, R. S. Brown, Inorg. Chem. 2004, 43, 6752.
-
(2004)
Inorg. Chem.
, vol.43
, pp. 6752
-
-
Desloges, W.1
Neverov, A.A.2
Brown, R.S.3
-
14
-
-
28444486973
-
-
R. E. Lewis, A. A. Neverov, R. S. Brown, Org. Biomol. Chem. 2005, 3, 4082.
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 4082
-
-
Lewis, R.E.1
Neverov, A.A.2
Brown, R.S.3
-
15
-
-
0042329190
-
-
For the designation of "pH" in methanol and measurement thereof, see: G. T. T. Gibson, A. A. Neverov, R. S. Brown, Can. J. Chem. 2003, 81, 495;
-
(2003)
Can. J. Chem.
, vol.81
, pp. 495
-
-
Gibson, G.T.T.1
Neverov, A.A.2
Brown, R.S.3
-
16
-
-
0000281034
-
-
spH in methanol is 8.4; E. Bosch, F. Rived, M. Rosés, J. Sales, J. Chem. Soc. Perkin Trans. 1 1999, 2, 1953.
-
(1999)
J. Chem. Soc. Perkin Trans. 1
, vol.2
, pp. 1953
-
-
Bosch, E.1
Rived, F.2
Rosés, M.3
Sales, J.4
-
17
-
-
29844455329
-
-
C. Maxwell, A. A. Neverov, R. S. Brown, Org. Biomol. Chem. 2005, 3, 4329.
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 4329
-
-
Maxwell, C.1
Neverov, A.A.2
Brown, R.S.3
-
18
-
-
33746273031
-
-
note
-
3+-catalyzed methanolysis of 5a must be essentially complete early in the NMR experiment because if it were not the summation of the 256 scans over five minutes would have revealed the presence of starting material in the first few scans.
-
-
-
-
19
-
-
33746285898
-
-
note
-
sPH 9.1.
-
-
-
-
20
-
-
33746306876
-
-
note
-
-1.
-
-
-
-
21
-
-
11844261429
-
-
The predicted rate constants assume that the Brønsted relationships of Equations (2) and (3), which are derived for aryl thiols, are followed by a primary alkyl thiol. Previous studies indicate that methanolysis and hydrolysis of carboxylate esters bearing aryloxy groups are up to tenfold less reactive than those bearing primary alkoxyl groups, presumably because of steric effects; see: a) N. E. Sunderland, A. A. Neverov, R. S. Brown, Org. Biomol. Chem. 2005, 3, 65;
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 65
-
-
Sunderland, N.E.1
Neverov, A.A.2
Brown, R.S.3
-
23
-
-
0030272334
-
-
P. Gans, A. Sabatini, A. Vacca, Talanta 1996, 43, 1739.
-
(1996)
Talanta
, vol.43
, pp. 1739
-
-
Gans, P.1
Sabatini, A.2
Vacca, A.3
|